人骨髓间充质干细胞体外转染血管内皮生长因子基因的实验研究

Dewu Liu, Xiangrong Zhang, Guanghua Guo, Yan Peng
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引用次数: 1

摘要

血管内皮生长因子165 (VEGF165)是最重要的血管生长因子之一,具有通过促进毛细血管再生来加速伤口愈合的潜力。然而,生长因子的生物半衰期短,严重制约了其临床应用。本研究旨在探讨转染VEGF165基因的人骨髓间充质干细胞(MSCs)的可行性和安全性,以期为今后临床皮肤修复提供一种新的方法。采用密度梯度离心和黏附相结合的方法分离纯化MSCs。通过脂质体介导转染将pShuttle-CMV/VEGF165引入培养的MSCs。分别采用逆转录聚合酶链反应(RT-PCR)、酶联免疫吸附试验(ELISA)和western blot检测转染MSCs和未转染MSCs中VEGF165基因和蛋白的表达。我们发现转染的MSCs中VEGF165 mRNA和蛋白的表达量远高于未转染的MSCs。结果表明,脂质体介导的血管内皮生长因子165基因可以成功转染人骨髓间充质干细胞。本研究为利用VEGF165基因转染加速组织工程皮肤移植血管化奠定了基础。
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Experimental Study of Human Bone Marrow Mesenchymal Stem Cells Transfected with Vascular Endothelial Growth Factor Gene in Vitro
Vascular endothelial growth factor 165 (VEGF165) is one of the most prominent vascular growth factors that has the potential to accelerate wound healing by promoting the regeneration of capillary vasculature. However, the short biological half-live of growth factors may impose severe restraints on their clinical applications. Here, we investigate the feasibility and safety of human bone marrow derived mesenchymal stem cells (MSCs) transfected with VEGF165 gene so as to provide a new method for clinical skin repair in the future. The MSCs were harvested, isolated and purified by combining density gradient centrifugation with adhering method. The pShuttle-CMV/VEGF165 was introduced into cultured MSCs through liposome-mediated transfection. The VEGF165 gene and protein expression in transfected MSCs and untransfected MSCs were determined by reverse transcription-polymerase chain reaction (RT-PCR), Enzyme-linked Immunoadsorbent Assay (ELISA) and western blot analysis respectively. We found that the expression of VEGF165 mRNA and protein in transfected MSCs were much higher than those in the untransfected MSCs. These results suggest that human bone marrow derived mesenchymal stem cells can be successfully transfected with vascular endothelial growth factor 165 gene mediated by liposome in vitro. The present study has laid a foundation for potential use of VEGF165 gene transfection to accelerate the vascularization of tissue engineered skins grafting.
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